A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391931



Internal ID21049484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73832201..73841000hg38UCSC Ensembl
chr4:74697918..74706717hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212353
Samples
Known GenesCXCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391931
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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